| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1021753944 |
| P356 | DOI | 10.1038/NG0595-67 |
| P698 | PubMed publication ID | 7647794 |
| P50 | author | Richard M. Durbin | Q4583003 |
| Sarah Baxendale | Q51838254 | ||
| Gos Micklem | Q30347699 | ||
| Greg Elgar | Q30519112 | ||
| P2093 | author name string | G Bates | |
| S Beck | |||
| S Brenner | |||
| S Abdulla | |||
| D Buck | |||
| M Berks | |||
| P2860 | cites work | DNA sequencing with chain-terminating inhibitors | Q22066207 |
| A novel G protein-coupled receptor kinase gene cloned from 4p16.3 | Q24337701 | ||
| Improved tools for biological sequence comparison | Q24652199 | ||
| Basic local alignment search tool | Q25938991 | ||
| A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 | ||
| Cloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplification | Q28118724 | ||
| DNA sequence analysis of 66 kb of the human MHC class II region encoding a cluster of genes for antigen processing | Q28208169 | ||
| CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 | Q28235526 | ||
| The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family | Q28240104 | ||
| The murine homologues of the Huntington disease gene (Hdh) and the alpha-adducin gene (Add1) map to mouse chromosome 5 within a region of conserved synteny with human chromosome 4p16.3 | Q28240728 | ||
| Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) | Q28250990 | ||
| A conserved retinoic acid response element required for early expression of the homeobox gene Hoxb-1. | Q52215015 | ||
| Random cloning and sequencing by the M13/dideoxynucleotide chain termination method. | Q54769070 | ||
| Striking sequence similarity over almost 100 kilobases of human and mouse T–cell receptor DNA | Q58515580 | ||
| Detection of rare mRNAs via quantitative RT-PCR | Q68024337 | ||
| Speculations on RNA splicing | Q70756413 | ||
| Automated DNA hybridization | Q72113876 | ||
| The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease | Q28264134 | ||
| Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | Q28273791 | ||
| Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene | Q28285882 | ||
| 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans | Q29547793 | ||
| Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries | Q33530293 | ||
| A fundamental division in the Alu family of repeated sequences | Q33585450 | ||
| A study of the Huntington's disease associated trinucleotide repeat in the Scottish population. | Q33596076 | ||
| Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. | Q33968674 | ||
| Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy | Q34023072 | ||
| Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15. | Q34346913 | ||
| Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. | Q34353488 | ||
| An unstable triplet repeat in a gene related to myotonic muscular dystrophy | Q34355359 | ||
| Mouse Huntington's disease gene homolog (Hdh). | Q34662498 | ||
| Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat | Q34662620 | ||
| Use of restriction enzymes to detect potential gene sequences in mammalian DNA. | Q35079757 | ||
| Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases | Q35442097 | ||
| A simple method for quantifying specific mRNAs in small numbers of early mouse embryos | Q35761592 | ||
| Triplet repeat mutations in human disease | Q36129554 | ||
| Smart2, a cosmid vector with a phage lambda origin for both systematic chromosome walking and P-element-mediated gene transfer in Drosophila | Q36421565 | ||
| Sequence of the murine Huntington disease gene: evidence for conservation, alternate splicing and polymorphism in a triplet (CCG) repeat [corrected] | Q36747904 | ||
| Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome | Q36754912 | ||
| A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene | Q36766598 | ||
| The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library | Q36783677 | ||
| Huntington's disease. Pathogenesis and management | Q39460676 | ||
| A sequence assembly and editing program for efficient management of large projects | Q40505372 | ||
| Non-methylated islands in fish genomes are GC-poor | Q40532504 | ||
| A strategy for the amplification, purification, and selection of M13 templates for large-scale DNA sequencing | Q41072384 | ||
| Nucleotide sequence of the BALB/c mouse beta-globin complex | Q42651379 | ||
| Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n | Q44229778 | ||
| Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms | Q45288525 | ||
| Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression | Q45289001 | ||
| Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5. | Q45289080 | ||
| Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence. | Q45289187 | ||
| Prototypic sequences for human repetitive DNA | Q48154904 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Huntington's disease | Q190564 |
| P304 | page(s) | 67-76 | |
| P577 | publication date | 1995-05-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | Comparative sequence analysis of the human and pufferfish Huntington's disease genes | |
| P478 | volume | 10 |
| Q34607539 | A functional role for some Fugu introns larger than the typical short ones: the example of the gene coding for ribosomal protein S7 and snoRNA U17. |
| Q45298821 | A putative Drosophila homolog of the Huntington's disease gene |
| Q61761316 | AP1 genes in Fugu indicate a divergent transcriptional control to that of mammals |
| Q41084183 | Aberrant processing of the Fugu HD (FrHD) mRNA in mouse cells and in transgenic mice |
| Q41658951 | Alu sequences |
| Q35021694 | Analysis of 148 kb of genomic DNA around the wnt1 locus of Fugu rubripes. |
| Q48037975 | Analysis of pufferfish homologues of the AT-rich human APP gene |
| Q24793605 | Analysis of the conservation of synteny between Fugu and human chromosome 12 |
| Q24620925 | Characterization of clustered MHC-linked olfactory receptor genes in human and mouse |
| Q22254320 | Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts |
| Q31987643 | Characterization of the Huntington's disease (HD) gene homologue in the zebrafish Danio rerio. |
| Q40962295 | Characterization of the transcription factor MTF-1 from the Japanese pufferfish (Fugu rubripes) reveals evolutionary conservation of heavy metal stress response |
| Q47945118 | Characterization of three genes, AKAP84, BAW and WSB1, located 3' to the neurofibromatosis type 1 locus in Fugu rubripes |
| Q52974959 | Classical and molecular cytogenetics of the pufferfish Tetraodon nigroviridis. |
| Q52900566 | Clonability and gene distribution on human chromosome 21: reflections of junk DNA content? |
| Q48041491 | Cloning and sequencing of complement component C9 and its linkage to DOC-2 in the pufferfish Fugu rubripes |
| Q40952719 | Comparative Analysis of Vertebrate Dystrophin Loci Indicate Intron Gigantism as a Common Feature |
| Q34734536 | Comparative analysis and genomic structure of the tuberous sclerosis 2 (TSC2) gene in human and pufferfish |
| Q42653078 | Comparative analysis of the ETV6 gene in vertebrate genomes from pufferfish to human. |
| Q38557041 | Computational gene discovery and human disease |
| Q37714624 | Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus) |
| Q77724522 | Counting on comparative maps |
| Q27766897 | Crystal structure of a dimeric chymotrypsin inhibitor 2 mutant containing an inserted glutamine repeat |
| Q73857884 | Cytogenetic analysis of the pufferfish Tetraodon fluviatilis (Osteichthyes) |
| Q77630835 | Cytogenetic and molecular analysis of the pufferfish Tetraodon fluviatilis (Osteichthyes) |
| Q30437121 | Deletion of the huntingtin polyglutamine stretch enhances neuronal autophagy and longevity in mice. |
| Q30425063 | Deletion of the huntingtin proline-rich region does not significantly affect normal huntingtin function in mice |
| Q28510315 | Deletion of the triplet repeat encoding polyglutamine within the mouse Huntington's disease gene results in subtle behavioral/motor phenotypes in vivo and elevated levels of ATP with cellular senescence in vitro |
| Q50737253 | Evidence for dynamic and multiple roles for huntingtin in Ciona intestinalis. |
| Q48795581 | Expression and distribution of the dentatorubral-pallidoluysian atrophy gene product (atrophin-1/drplap) in neuronal and non-neuronal tissues |
| Q39758710 | Faithful expression of a tagged Fugu WT1 protein from a genomic transgene in zebrafish: efficient splicing of pufferfish genes in zebrafish but not mice |
| Q33957062 | Fugu: a compact vertebrate reference genome |
| Q71990830 | Gain of glutamines, gain of function? |
| Q27023050 | Genetics and neuropathology of Huntington's disease |
| Q45254653 | Genomic characterization of the Neurofibromatosis Type 1 gene of Fugu rubripes |
| Q40414290 | Genomic sequence analysis of Fugu rubripes CFTR and flanking genes in a 60 kb region conserving synteny with 800 kb of human chromosome 7. |
| Q24626326 | Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1 |
| Q41312696 | Glutamine repeats and inherited neurodegenerative diseases: molecular aspects |
| Q41941047 | Glutamine repeats as polar zippers: their role in inherited neurodegenerative disease |
| Q28185534 | Growth hormone secretagogue receptor family members and ligands |
| Q48061984 | Human lipoprotein lipase last exon is not translated, in contrast to lower vertebrates |
| Q33263046 | Huntingtin gene evolution in Chordata and its peculiar features in the ascidian Ciona genus |
| Q45296265 | Huntingtin: a single bait hooks many species |
| Q38578817 | Huntington's disease: from gene to potential therapy. |
| Q57178431 | Huntington's disease: the coming of age |
| Q41235542 | Huntington's disease: translating a CAG repeat into a pathogenic mechanism |
| Q28202315 | Intron loss in the SART1 genes of Fugu rubripes and Tetraodon nigroviridis |
| Q34504653 | Intron-exon structures of eukaryotic model organisms |
| Q36535666 | Is Huntington's a glutamine storage disease? |
| Q48039226 | Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripes |
| Q36224691 | Mapping of complex regulatory elements by pufferfish/zebrafish transgenesis |
| Q41202056 | Modern genome research and DNA diagnostics in domestic animals in the light of classical breeding techniques |
| Q47822200 | Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis. |
| Q58052547 | More genes in fish? |
| Q48207865 | Neural expression of the Huntington's disease gene as a chordate evolutionary novelty. |
| Q28281904 | Normal huntingtin function: an alternative approach to Huntington's disease |
| Q48291079 | Pathogenesis of neurodegenerative diseases associated with expanded glutamine repeats: new answers, new questions. |
| Q40407355 | Pressing ahead with human genome sequencing |
| Q37714529 | Pufferfish and new paradigm for comparative genome analysis |
| Q40957100 | Quality not quantity: the pufferfish genome |
| Q42177238 | Repertoire of Protein Kinases Encoded in the Genome of Takifugu rubripes |
| Q38328628 | Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes |
| Q37969749 | The biological function of the Huntingtin protein and its relevance to Huntington's Disease pathology |
| Q37348589 | The conserved role of Krox-20 in directing Hox gene expression during vertebrate hindbrain segmentation. |
| Q41456204 | The genetic defect causing Huntington's disease: repeated in other contexts? |
| Q48281209 | The mitochondrial genome of the pufferfish, Fugu rubripes, and ordinal teleostean relationships |
| Q30429568 | The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish Fugu |
| Q42174981 | The role of intrinsically unstructured proteins in neurodegenerative diseases |
| Q42061847 | Towards a reconciliation of the introns early or late views: triosephosphate isomerase genes from insects |
| Q48357496 | Transgenic mice in the study of polyglutamine repeat expansion diseases |
| Q24676606 | Transgenic models of Huntington's disease |
| Q37407466 | Translocation events in the evolution of aminoacyl-tRNA synthetases. |
| Q37249765 | Trends in the molecular pathogenesis and clinical therapeutics of common neurodegenerative disorders |
| Q47990453 | Triplet repeat variability in the signal peptide sequence of the Xmrk receptor tyrosine kinase gene in Xiphophorus fish |
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